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- Tasks: Manage on-site monitoring and ensure compliance with clinical trial protocols.
- Company: Global leader in clinical research services with a commitment to innovation.
- Benefits: Competitive salary, travel opportunities, and professional development.
- Why this job: Make a real difference in healthcare by ensuring clinical trials run smoothly.
- Qualifications: Life science degree and experience in managing clinical trials.
- Other info: Dynamic role with travel to various clinical sites across the UK.
The predicted salary is between 36000 - 60000 £ per year.
A global provider of clinical research services is seeking an experienced Clinical Research Associate to manage on-site monitoring and ensure compliance with regulatory requirements. Ideal candidates will have a life science degree and experience managing multiple clinical trial protocols.
Responsibilities include:
- Monitoring visits
- Evaluating site practices
- Maintaining documentation standards
This full-time role is based in Reading, Berkshire, with travel required to various clinical sites.
Senior Clinical Research Associate - Field Monitoring (UK) in London employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate - Field Monitoring (UK) in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for those interviews by brushing up on your knowledge of regulatory requirements and clinical trial protocols. We recommend doing mock interviews with friends or using online resources to get comfortable with common questions.
✨Tip Number 3
Showcase your experience! When you get the chance to meet potential employers, be ready to discuss specific examples from your past roles that highlight your skills in monitoring visits and maintaining documentation standards.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing familiar faces in our candidate pool!
We think you need these skills to ace Senior Clinical Research Associate - Field Monitoring (UK) in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in clinical trials and monitoring. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant skills and achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical research and how your life science degree has prepared you for this role. Let us know what makes you the perfect fit!
Showcase Your Compliance Knowledge: Since compliance is key in this role, make sure to mention any specific regulations or guidelines you’re familiar with. We love candidates who can demonstrate their understanding of the regulatory landscape!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates during the process!
How to prepare for a job interview at IQVIA LLC
✨Know Your Clinical Trials
Make sure you brush up on the latest clinical trial protocols and regulations. Being able to discuss specific trials you've managed or monitored will show your expertise and confidence in the field.
✨Showcase Your Compliance Knowledge
Prepare to talk about how you've ensured compliance with regulatory requirements in past roles. Use examples that highlight your attention to detail and understanding of documentation standards.
✨Demonstrate Your Monitoring Skills
Be ready to discuss your approach to on-site monitoring visits. Share specific strategies you've used to evaluate site practices effectively, as this will demonstrate your hands-on experience and problem-solving abilities.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's clinical research processes and their expectations for the role. This shows your genuine interest in the position and helps you assess if it's the right fit for you.
